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限制蛋氨酸摄入可防止瘦素缺乏型肥胖小鼠的肝脂肪变性进展。

Methionine restriction prevents the progression of hepatic steatosis in leptin-deficient obese mice.

机构信息

Orentreich Foundation for the Advancement of Science, Inc., 855 Route 301, Cold Spring-on-Hudson, NY 10516, USA.

出版信息

Metabolism. 2013 Nov;62(11):1651-61. doi: 10.1016/j.metabol.2013.06.012. Epub 2013 Aug 5.

Abstract

OBJECTIVE

This study investigated the effects of dietary methionine restriction (MR) on the progression of established hepatic steatosis in the leptin-deficient ob/ob mouse.

MATERIAL/METHODS: Ten-week-old ob/ob mice were fed diets containing 0.86% (control-fed; CF) or 0.12% methionine (MR) for 14 weeks. At 14 weeks, liver and fat were excised and blood was collected for analysis. In another study, blood was collected to determine in vivo triglyceride (TG) and very-low-density lipoprotein (VLDL) secretion rates. Liver histology was conducted to determine the severity of steatosis. Hepatic TG, free fatty acid levels, and fatty acid oxidation (FAO) were also measured. Gene expression was analyzed by quantitative PCR.

RESULTS

MR reversed the severity of steatosis in the ob/ob mouse. This was accompanied by reduced body weight despite similar weight-specific food intake. Compared with the CF group, hepatic TG levels were significantly reduced in response to MR, but adipose tissue weight was not decreased. MR reduced insulin and HOMA ratios but increased total and high-molecular-weight adiponectin levels. Scd1 gene expression was significantly downregulated, while Acadvl, Hadha, and Hadhb were upregulated in MR, corresponding with increased β-hydroxybutyrate levels and a trend toward increased FAO. The VLDL secretion rate was also significantly increased in the MR mice, as were the mRNA levels of ApoB and Mttp. The expression of inflammatory markers, such as Tnf-α and Ccr2, was also downregulated by MR.

CONCLUSIONS

Our data indicate that MR reverses steatosis in the ob/ob mouse liver by promoting FAO, increasing the export of lipids, and reducing obesity-related inflammatory responses.

摘要

目的

本研究旨在探讨饮食蛋氨酸限制(MR)对肥胖症(ob/ob)小鼠肝脏脂肪变性进展的影响。

材料/方法:10 周龄的 ob/ob 小鼠分别喂食含 0.86%蛋氨酸(对照组;CF)或 0.12%蛋氨酸(MR)的饮食 14 周。14 周时,切除肝脏和脂肪组织,采集血液进行分析。另一项研究中,采集血液以确定体内甘油三酯(TG)和极低密度脂蛋白(VLDL)分泌率。进行肝脏组织学检查以确定脂肪变性的严重程度。还测量了肝 TG、游离脂肪酸水平和脂肪酸氧化(FAO)。通过定量 PCR 分析基因表达。

结果

MR 逆转了 ob/ob 小鼠脂肪变性的严重程度。尽管体重特异性食物摄入量相似,但体重减轻。与 CF 组相比,MR 组肝 TG 水平显著降低,但脂肪组织重量并未减少。MR 降低了胰岛素和 HOMA 比值,但增加了总和高分子量脂联素水平。Scd1 基因表达显著下调,而 Acadvl、Hadha 和 Hadhb 在 MR 中上调,对应于 β-羟丁酸水平增加和 FAO 增加的趋势。MR 还显著增加了 VLDL 分泌率,ApoB 和 Mttp 的 mRNA 水平也增加。MR 还下调了炎症标志物如 Tnf-α和 Ccr2 的表达。

结论

我们的数据表明,MR 通过促进 FAO、增加脂质输出和减少肥胖相关的炎症反应,逆转 ob/ob 小鼠肝脏的脂肪变性。

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